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Q38814847-4D615F0C-CE98-4F0D-8BD3-A7185CB2D316
Q38814847-4D615F0C-CE98-4F0D-8BD3-A7185CB2D316
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Statement
http://www.wikidata.org/entity/statement/Q38814847-4D615F0C-CE98-4F0D-8BD3-A7185CB2D316
Genetics of Frontotemporal Lobar Degeneration: From the Bench to the Clinic.
P2860
Q38814847-4D615F0C-CE98-4F0D-8BD3-A7185CB2D316
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38814847-4D615F0C-CE98-4F0D-8BD3-A7185CB2D316
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wasDerivedFrom
7faf8aaee58f0bb6da2421d21e7a77839f74430e
P2860
Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure.